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rs16910061

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs16910061(A;A)
Make rs16910061(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position94552459
is asnp
is mentioned by
dbSNPrs16910061
ebirs16910061
HLIrs16910061
Exacrs16910061
Varsomers16910061
Maprs16910061
PheGenIrs16910061
hapmaprs16910061
1000 genomesrs16910061
hgdprs16910061
ensemblrs16910061
gopubmedrs16910061
geneviewrs16910061
scholarrs16910061
googlers16910061
pharmgkbrs16910061
gwascentralrs16910061
openSNPrs16910061
23andMers16910061
23andMe allrs16910061
SNP Nexus

SNPshotrs16910061
SNPdbers16910061
MSV3drs16910061
GWAS Ctlgrs16910061
GMAF0.0753
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19893584]
Trait Height
Title Identification of 15 loci influencing height in a Korean population
Risk Allele T
P-val 0.000003
Odds Ratio 0.53 [NR] cm decrease


GET Evidence
rs16910061
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0546875
summary